You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Please see example attached. This is for a simulated read set of a single species, and a kmer collection containing that species amongst others. How is it possible for the number of unique reads in the results table to be greater than the number of reads used for the analysis?
Please see example attached. This is for a simulated read set of a single species, and a kmer collection containing that species amongst others. How is it possible for the number of unique reads in the results table to be greater than the number of reads used for the analysis?
report_ft2.zip
I have tried to use the -o parameter to output the reads that contain kmers from my collection, but it outputs an empty file.
I have run fastv as follows:
fastv -o FT.fastq -w 16 -c unique_kmer/kmercollection.fasta -q 10 -h ./all_pathogens_crs_results/report_ft2.html -j ./all_pathogens_crs_results/report_ft2.json -i ft_lt5k.fastq
The text was updated successfully, but these errors were encountered: